| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103562282-103562356 | Rare:30 | ||||
| chr14:103562623-103563048 | Common:8; Rare:166; Clinvar (benign):5 | ||||
| chr14:103629111-103629452 | Common:3; Rare:137 | ||||
| chr14:103715470-103715917 | Common:1; Rare:141 | ||||
| chr14:103742189-103742454 | Common:1; Rare:51 | ||||
| chr14:104752902-104753212 | Common:3; Rare:113 | ||||
| chr14:104776662-104777006 | Common:1; Rare:80; Clinvar:4; Clinvar (benign):4 | ||||
| chr14:104970465-104970798 | Common:4; Rare:64 | ||||
| chr14:104985628-104985806 | Common:3; Rare:69 | ||||
| chr14:105301300-105301567 | Rare:71 | ||||
| chr14:105476950-105477275 | Common:1; Rare:65 | ||||
| chr14:105487032-105487298 | Common:2; Rare:89 | ||||
| chr14:105487592-105487983 | Common:1; Rare:121 | ||||
| chr15:22838356-22838764 | Common:3; Rare:147 | ||||
| chr15:22980292-22980491 | Rare:73 |